Role of cell-type specific circuits in visual processing
Role of cell-type specific circuits in visual processing
批准号:
9195098
负责人:
David C Lyon
金额:
$37.67万
依托单位国家:
美国
项目类别:
财政年份:
2015
资助国家:
美国
项目状态:
已结题
起止时间:
2015-01-01 至 2018-12-31
关键词:
AddressAnimalsAutomobile DrivingBrainCell physiologyComplexFelis catusGenesGoalsHalorhodopsinsInjectableInjection of therapeutic agentLasersLateralLateral Geniculate BodyLinkMammalsMapsMeasuresMediatingMonkeysNeuronsNeurophysiology - biologic functionOpticsPlayRabies virusRecombinant adeno-associated virus (rAAV)RoleSeriesSignal TransductionStimulusStructureStructure-Activity RelationshipTechniquesTestingTransgenic MiceViralViral VectorVisionVisualVisual CortexVisual Fieldsarea striatacell typeexcitatory neuronexperimental studyhippocampal pyramidal neuronimprovedin vivoinhibitory neuroninnovationnoveloptical imagingoptogeneticsorientation selectivitypromoterpublic health relevancereceptive fieldresponseretinotopicselective expressionsuperior colliculus Corpora quadrigeminatoolvisual processvisual processingvisual stimulus
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): Specific cell types and their connectivity are a key determinant in neural function and selectivity. Primary visual cortex (V1) is one of the largest and most complex structures in the brain and several recent technological advances have enabled more detailed probing of cell type specific relationships to connectivity for a range of V1
cell functions, including orientation selectivity, aperture tuning, contrast response functions, an gain control. Nevertheless, technical limitations remain that have largely limited these studies to
transgenic mice which lack more complex organization found in higher visual species like cat and monkey. We recently developed viral strategies for accessing specific cell types and specific circuits in non-transgenic species (Liu et al., 2013, Curr Biol) opening the door for unprecedented fine scale study of structure-function relationships in highly visual mammals. For this proposal we will apply these new strategies to enable optogenetic manipulation of specific cell types and circuits in cat V1, including superficial layer inhibitory neurons (Aim 1), long-ran lateral inputs to superficial inhibitory neurons (Aim 2), and layer 5 and 6 subcortical projection neurons that directly (or indirectly) interact with superficial layer neurons (Aim 3). Specific questions that we will address include whether and how orientation selectivity and surround suppression interact and are mediated by each of these circuits. These studies will represent the most direct in vivo assessment of inhibitory neurons and underlying intra- and inter-laminar circuitry of a large, highly visual mammal, advancing our understanding of how basic visual processes arise and depend on complex cortical structure.
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会议论文
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批准号:10446188
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资助金额:$59.51万
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财政年份:2022
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负责人:David C Lyon
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Retinal sheet transplant impact on functional organization of visual cortex in retinal degenerate animal models
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批准号:10057749
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财政年份:2020
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Role of cell-type specific circuits in visual processing
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批准号:8799987
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资助金额:$37.78万
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财政年份:2015
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Cell Type Specific Tracing of Neocortical Circuits Using Viral Vectors
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资助金额:$24.41万
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财政年份:2012
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Cell Type Specific Tracing of Neocortical Circuits Using Viral Vectors
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资助金额:$19.23万
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财政年份:2012
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Contextual modulation of orientation specificity in V1
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批准号:6665280
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财政年份:2002
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Contextual modulation of orientation specificity in V1
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批准号:6584065
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资助金额:$3.83万
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财政年份:2002
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Contextual modulation of orientation specificity in V1
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批准号:6897366
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项目类别:
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资助金额:$0.97万
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财政年份:2002
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Contextual modulation of orientation specificity in V1
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批准号:6797339
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项目类别:
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资助金额:$4.89万
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财政年份:2002
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负责人:David C Lyon
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依托单位:
海外基金